Intelligence · Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors — phase, modality, and trial IDs for BD and competitive intelligence.
- Programs indexed
- 20,548
- Companies
- 1,769
- Drugs tracked
- 4,797
Quick answer
NovaPharmaNews tracks 20,548 pharmaceutical R&D pipeline programs sourced from ClinicalTrials.gov, linked to sponsor companies. Each profile includes development phase, modality, trial status, NCT identifiers, and indication text — searchable for business development and competitive intelligence.
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Antihemophilic Factor Manufactured and Formulated without Added Human or Animal Proteins (rAHF-PFM)
Takeda
Hemophilia A
1 trial -
Antiplatelet (Aspirin, Dipyridamole, clopidogrel)
United Therapeutics Europe Ltd
Cervical Artery Dissection
1 trial -
Apitox, purified honeybee toxin, lyophilized in saline
Apimeds Pharmaceuticals US
Osteoarthritis of the Knee
1 trial -
Apixaban
United Therapeutics Europe Ltd
Cerebral Vein Thrombosis
2 trials -
Apremilast, Apremilast, Apremilast
Amgen
Behçet’s disease is a chronic, relapsing, multisystem inflammatory disorder of unknown etiology characterized by 4 major symptoms (oral aphthous ulcers, genital ulcers, skin lesions, and ocular lesions) and occasionally by 5 minor symptoms (arthritis, gastrointestinal ulcers, epididymitis, vascular lesions, and central nervous system [CNS] symptoms) (Cho, 2012). Juvenile idiopathic arthritis is a heterogeneous group of chronic inflammatory disorders that initially presents in children by the age of 16 years. It refers to arthritis of at least 6 weeks duration of unknown etiology that begins in children less than 16 years old. Juvenile idiopathic arthritis has an annual incidence of 2 to 20 cases per 100 000 population and a prevalence of 16 to 150 cases per 100 000 population. It is an autoimmune disorder marked by abnormalities of immune responses (Adelowo, 2010).
1 trial -
Apremilast, Apremilast, Apremilast, Apremilast placebo product is supplied to the clinic as 10, 20 and 30 mg tablets and 5 mg/mL oral solution. The placebo product is the same as the drug product formulation except there is no active apremilast., Apremilast
Amgen
Juvenile psoriatic arthritis
1 trial -
Aramchol free acid
Galmed Pharmaceuticals
Nonalcoholic Steatohepatitis (NASH)
1 trial -
Aromatase Inhibitors
United Therapeutics Europe Ltd
Breast Cancer
1 trial -
Artemether-lumefantrine
AVENUE THERAPEUTICS, INC.
Plasmodium Falciparum Malaria
1 trial -
Aspirin
United Therapeutics Europe Ltd
Node Positive HER2 Negative Breast Cancer
1 trial -
Aspirin 75 mg daily
Century Therapeutics
Intracerebral Haemorrhage
1 trial -
Astragalus Membranaceus
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Aneurysmal Subarachnoid Hemorrhage
1 trial -
Asundexian (BAY2433334)
Bayer HealthCare AG
Prevention of Stroke or Systemic Embolism
1 trial -
Asundexian (BAY2433334)
Bayer HealthCare AG
Prevention of Ischemic Stroke
1 trial -
Atacicept
Vera Therapeutics
IgA Nephropathy
1 trial -
Atacicept
Vera Therapeutics
Lupus Nephritis (LN)
1 trial -
Ataluren
PTC THERAPEUTICS, INC.
Muscular Dystrophy, Duchenne
3 trials -
Ataluren
PTC THERAPEUTICS, INC.
Duchenne Muscular Dystrophy
9 trials -
Ataluren
PTC THERAPEUTICS, INC.
Cystic Fibrosis
6 trials -
Ataluren (PTC124®)
PTC THERAPEUTICS, INC.
Cystic Fibrosis
1 trial -
Atenativ 1000 I.E. - Pulver und Lösungsmittel zur Herstellung einer Injektions- oder Infusionslösung, Atenativ, 50 IU/ml, práek a rozpoutědlo pro infuzní roztok, Atenativ 500 I.E. - Pulver und Lösungsmittel zur Herstellung einer Injektions- oder Infusionslösung, Atenativ 50 i.e./ml praek in vehikel za raztopino za infundiranje, Atenativ 50 IU/ml prášek a rozpouštědlo pro infuzní roztok, ATENATIV 50 UI/mL, poudre et solvant pour solution pour perfusion, ATENATIV 50 UI/mL, poudre et solvant pour solution p
Lacuna Pharma Pty Ltd
Acquired Antithrombin Deficiency (Heparin Resistance)
1 trial -
Atezolizumab
Hoffmann-La Roche
Melanoma
1 trial -
Atezolizumab
Hoffmann-La Roche
Breast Cancer
1 trial -
Atezolizumab
Hoffmann-La Roche
Carcinoma, Hepatocellular
1 trial
Frequently asked questions
What is the NovaPharmaNews pipeline directory?
It is a searchable index of 20,548 clinical development programs grouped by sponsor company, with phase (Phase 1–3), modality, trial status, and linked NCT IDs from ClinicalTrials.gov.
Where does pipeline data come from?
Program records are derived from ClinicalTrials.gov and linked to NovaPharmaNews company profiles. Trial status and phase reflect registry data at last sync — verify on ClinicalTrials.gov before investment or partnering decisions. See our data sources page for attribution.
How do I find pipeline programs by company or phase?
Use the search box to match program name, indication, company name, or slug. Results are ordered with late-stage (Phase 3) programs first. Open any row to view the full program profile under its sponsor company.
Data attribution and licensing: Data sources